Thomas Peterson

Senior Clinical Research Associate @Advanced Clinical

Independently execute all activities related to a clinical study, including (but not limited to)-Clinical site selection-Site contract and budget negotiation. Study initiation visits-Interim monitoring visits-Study close out visits-Data monitoring activities, including on-site and remote audits of study data for accuracy, integrity, and completeness-Identify and suggest ways to resolve problems or issues which could affect the integrity of the data or timely completion of the clinical study-Prepare and/or review study protocols and study documents for new and modified products-Prepare and/or review clinical reports and applicable sections of regulatory submissions and scientific abstracts, posters, and publications-May serve as the clinical affairs representative on a project team-Maintain a high level of familiarity with clinical literature in the field of study and related areas and stay up to date on major advances in disease diagnosis and/or detection and the use of new tests and advances in clinical practice.